1. NT-PROBNP as a screening tool for low-risk patent ductus arteriousus: a follow-up validation study.
- Author
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López-Blanco G, Oulego-Erroz I, Pou-Blázquez Á, Medina-Guerrero C, Rodríguez-Blanco S, Alonso-Quintela P, Pérez-Muñuzuri A, and Couce-Pico ML
- Subjects
- Infant, Infant, Newborn, Humans, Follow-Up Studies, Biomarkers, Natriuretic Peptide, Brain, Infant, Premature, Ductus Arteriosus, Patent diagnostic imaging
- Abstract
The purpose of the study is to test whether NT-proBNP serves as a screening tool for low-risk patent ductus arteriosus and safely avoids routine early echocardiography. This is a prospective observational study in preterm infants ≤32 weeks of gestational age. Infants with ≥5100 pg/ml (positive screening) at 48-72 hours of life received comprehensive echocardiography and were treated according to shunt severity. Infants with NT-proBNP below 5100 pg/ml (negative screening) were managed expectantly. The main outcome was need for ductus treatment within the first 7 days of life. One hundred twenty-five infants were included; 82 had a negative NT-proBNP screening and 43 had a positive NT-proBNP screening. No infant (0%) with a negative screening was treated for ductus while 26 (60.4%) with a positive screening were treated (p < 0.001). NT-proBNP avoided a 65.6% of routine echocardiograms. NT-proBNP had an excellent performance to predict PDA treatment (AUC = 0.967).Conclusion: NT-proBNP at 48-72 hours of life has an excellent performance to detect low risk and avoids unnecessary echocardiograms. This may contribute to optimize PDA management in terms of resource utilization., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Published
- 2023
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